A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834436



Internal ID16128392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104680242..104742230hg38UCSC Ensembl
Innerchr14:105146579..105208567hg19UCSC Ensembl
Innerchr14:104217624..104279612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3861989
hg1961989
hg1861989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566055
Supporting Variants
Samples
Known GenesADSSL1, INF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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